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Cerebroretinal microangiopathy with calcifications and cysts 1

MONDO:0024564

Any Coats plus syndrome in which the cause of the disease is a mutation in the CTC1 gene.

Also known as: cerebroretinal microangiopathy with calcifications and cysts, CTC1 Coats plus syndrome, Coats plus syndrome caused by mutation in CTC1, cerebroretinal microangiopathy with calcifications and cysts 1, CRMCC1, Coats plus syndrome, Crmcc

24 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Eye disorder (97) Retinal disorder (79) Human disease (14) Telomere syndrome (9) Premature aging syndrome (6) Hereditary neurological disease (5) Disorder of orbital region (3)
Trials to join now! 16 Not yet recruiting 1 Not yet finished but already full! 2 Completed 4 Terminated 1
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  • New eye camera could spot retinal disease earlier

    Knowledge-focused Not yet recruiting

    This study will test a new, noninvasive camera called XyCAM CRE that measures blood flow in the back of the eye. Researchers will compare its images with standard eye tests in 350 adults with retinal disorders. The goal is to see if this camera can provide extra information to he…

    Sponsor: Stuart Terry Eye Associates • Aim: Knowledge-focused

    Last updated Jun 27, 2026 13:07 UTC

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